Canonical Allele Identifier: CA9201115

Gene: DNM2

Linked Data

• dbSNP Id: rs767092333
• ExAC: 19:10909131 G / A
• gnomAD v2: 19-10909131-G-A
• gnomAD v4: 19-10798455-G-A
• MyVariant Identifiers: chr19:g.10909131G>A (hg19) ; chr19:g.10798455G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10798455G>A , CM000681.2:g.10798455G>A	GRCh38
NC_000019.9:g.10909131G>A , CM000681.1:g.10909131G>A	GRCh37
NC_000019.8:g.10770131G>A	NCBI36
NG_008792.1:g.85377G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682285.1:n.1524-31G>A
ENST00000683738.1:n.1663-31G>A
ENST00000355667.11:c.1336-31G>A	ENSP00000347890.6:n.1336-31G>A
ENST00000389253.9:c.1336-31G>A MANE Select	ENSP00000373905.4:n.1336-31G>A
ENST00000355667.10:c.1336-31G>A	ENSP00000347890.6:n.1336-31G>A
ENST00000359692.10:c.1336-31G>A	ENSP00000352721.6:n.1336-31G>A
ENST00000389253.8:c.1336-31G>A	ENSP00000373905.3:n.1336-31G>A
ENST00000408974.8:c.1336-31G>A	ENSP00000386192.3:n.1336-31G>A
ENST00000585892.5:c.1336-31G>A	ENSP00000468734.1:n.1336-31G>A
ENST00000587329.1:n.69G>A
ENST00000587830.2:c.592-31G>A	ENSP00000466603.2:n.592-31G>A
ENST00000593220.1:n.485-31G>A
NM_001005360.2:c.1336-31G>A	NP_001005360.1:n.1336-31G>A
NM_001005361.2:c.1336-31G>A	NP_001005361.1:n.1336-31G>A
NM_001005362.2:c.1336-31G>A	NP_001005362.1:n.1336-31G>A
NM_001190716.1:c.1336-31G>A	NP_001177645.1:n.1336-31G>A
NM_004945.3:c.1336-31G>A	NP_004936.2:n.1336-31G>A
NM_001005361.3:c.1336-31G>A MANE Select	NP_001005361.1:n.1336-31G>A
NM_001190716.2:c.1336-31G>A	NP_001177645.1:n.1336-31G>A
NM_001005360.3:c.1336-31G>A	NP_001005360.1:n.1336-31G>A
NM_001005362.3:c.1336-31G>A	NP_001005362.1:n.1336-31G>A
NM_004945.4:c.1336-31G>A	NP_004936.2:n.1336-31G>A